Official recall notice

FDA DeviceClass IINotable

Single USE Tourniquet Cuff 30 2 Line Recall (Oct 2026)

Product: Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30" 2 LINE (10) Model/Catalog Number: DT-7030-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No

Recall date
2026-10-07
FDA class
Class II

Why it was recalled

Hazard

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.

One email a week when there are new recalls. Confirm by email; unsubscribe anytime.

Product description

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.

Affected products

Lot Code: Model Number: DT-7030-02Q UDI-DI: UDI was not applicable at time of manufacture. All Lots produced from 01SEP2016 to 01MAR2023: S1101STY, R1201STY, Q1115STY, O1020STY, N0330STY, N0530STY, N0730STY

Related Recalls